FSP Medical Writer

at  Thermo Fisher Scientific

EDUCATION AND EXPERIENCE:

Bachelor’s degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years of regulatory writing).
Experience working in the pharmaceutical/CRO industry preferred.
Experience in scientific writing advantageous.
Experience in the therapeutic areas of Immunology, Oncology or Vaccines advantageous.

KNOWLEDGE, SKILLS, AND ABILITIES:

• Solid medical writing skills, including grammatical, editorial, and proofreading skills.
• Ability to interpret and present complex data accurately and concisely.
• Effective administrative, organizational, and planning skills; attention to detail and quality
• Ability to work on own initiative and effectively within a team.
• Effective oral and written communication skills
• Good knowledge of regulatory documentation and drug development process
• Great judgment and decision-making skills
• Good computer skills and skilled with client templates; Good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook)

SUMMARIZED PURPOSE:

We are excited to expand our Philippines Medical Writing FSP Team! We are looking for a Medical Writer to join our team in the FSP space; experience in Immunology, Oncology or Vaccines would be valuable but not essential. The writer will provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. You will collaborate with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.

ESSENTIAL FUNCTIONS:

• Serves as primary author who writes and provides input on routine documents such as clinical study reports and study protocols and summarizes data from clinical studies.
• May assist with more complex clinical and scientific and program level documents, including IBs, INDs, and MAAs.
• Ensures compliance with quality processes and requirements for assigned documents. May assist in determining best practices, methods, and techniques for achieving optimal results.
• May assist in program management activities. Duties could include assisting with developing timelines, budgets, forecasts for assigned deliverables.
• Represents the department at project launch meetings, review meetings, and project team meetings.